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Trs20, Trs23, Trs31 and Bet5 participate in autophagy through GTPase Ypt1 in Saccharomyces cerevisiae

机译:Trs20,Trs23,Trs31和Bet5通过GTPase Ypt1参与酿酒酵母中的自噬。

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TRAPP (transport protein particle) is a large, highly conserved, multi-subunit complex. Four types of TRAPP complexes (I, II, III and most recently IV) have been identified in Saccharomyces cerevisiae . Studies on the roles of TRAPP II, TRAPP III and TRAPP IV specific subunits (Trs130, Trs85 and Trs33) have demonstrated that TRAPP II, TRAPP III and TRAPP IV activate the small GTPases that regulate autophagy. Up to now, the roles of the common TRAPP subunits have been well studied in vesicle transport. However, the roles of the common TRAPP subunits and their relationship to Ypt/Rab GTPases in autophagy are not clear. In this paper, we examined Trs20, Trs23, Trs31, and Bet5 (the common TRAPP subunits), which are required for starvation-induced autophagy and the cytoplasm-to-vacuole targeting (Cvt) pathway. During autophagy, GFP-Atg8 accumulates as single or multiple dots and is not recruited into the pre-autophagosomal structures (PAS) in trs20ts , trs23ts , trs31ts and bet5ts mutant cells. Furthermore, these dots are linked to the endoplasmic reticulum in mutant cells. Additionally, overexpression of Ypt1, but not Ypt31, suppresses the autophagy defect in trs20ts , trs23ts , trs31ts and bet5ts mutant cells. Based on these results, we concluded that Trs20, Trs23, Trs31, and Bet5 are required for autophagy, and that these common TRAPP subunits regulate autophagy partially through GTPase Ypt1, but not Ypt31.https://doi.org/10.2298/ABS170408030ZReceived: April 8, 2017; Revised: June 20, 2017; Accepted: July 29, 2017; Published online: August 28, 2017How to cite this article: Zou S, Liu Y, Min G, Liang Y. Trs20, Trs23, Trs31 and Bet5 participate in autophagy through GTPase Ypt1 in Saccharomyces cerevisiae . Arch Biol Sci. 2018;70(1):109-18.
机译:TRAPP(运输蛋白颗粒)是一个大型,高度保守的多亚基复合物。在酿酒酵母中已鉴定出四种类型的TRAPP复合物(I,II,III和最近的IV)。关于TRAPP II,TRAPP III和TRAPP IV特定亚基(Trs130,Trs85和Trs33)的作用的研究表明,TRAPP II,TRAPP III和TRAPP IV激活了调节自噬的小GTPase。到目前为止,在囊泡运输中已经很好地研究了常见的TRAPP亚基的作用。但是,尚不清楚自噬中常见的TRAPP亚基的作用及其与Ypt / Rab GTPases的关系。在本文中,我们研究了饥饿诱导的自噬和细胞质-液泡靶向(Cvt)途径所需的Trs20,Trs23,Trs31和Bet5(常见的TRAPP亚基)。在自噬过程中,GFP-Atg8会以单个或多个点的形式累积,并且不会被募集到trs20ts,trs23ts,trs31ts和bet5ts突变细胞的自噬前体结构(PAS)中。此外,这些点与突变细胞中的内质网相连。此外,Ypt1而不是Ypt31的过表达抑制了trs20ts,trs23ts,trs31ts和bet5ts突变细胞中的自噬缺陷。根据这些结果,我们得出结论,自噬需要Trs20,Trs23,Trs31和Bet5,并且这些常见的TRAPP亚基部分通过GTPase Ypt1而不是Ypt31调节自噬.https://doi.org/10.2298/ABS170408030Z 2017年4月8日;修订日期:2017年6月20日;接受:2017年7月29日;在线发布:2017年8月28日如何引用本文:邹S,刘Y,闵G,梁Y.Trs20,Trs23,Trs31和Bet5通过GTPase Ypt1参与酿酒酵母中的自噬。 Arch Biol科学。 2018; 70(1):109-18。

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